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Wnt/β-catenin Signaling in Cancers and Targeted Therapies

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Date 2021 Aug 30
PMID 34456337
Citations 220
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Abstract

Wnt/β-catenin signaling has been broadly implicated in human cancers and experimental cancer models of animals. Aberrant activation of Wnt/β-catenin signaling is tightly linked with the increment of prevalence, advancement of malignant progression, development of poor prognostics, and even ascendence of the cancer-associated mortality. Early experimental investigations have proposed the theoretical potential that efficient repression of this signaling might provide promising therapeutic choices in managing various types of cancers. Up to date, many therapies targeting Wnt/β-catenin signaling in cancers have been developed, which is assumed to endow clinicians with new opportunities of developing more satisfactory and precise remedies for cancer patients with aberrant Wnt/β-catenin signaling. However, current facts indicate that the clinical translations of Wnt/β-catenin signaling-dependent targeted therapies have faced un-neglectable crises and challenges. Therefore, in this study, we systematically reviewed the most updated knowledge of Wnt/β-catenin signaling in cancers and relatively targeted therapies to generate a clearer and more accurate awareness of both the developmental stage and underlying limitations of Wnt/β-catenin-targeted therapies in cancers. Insights of this study will help readers better understand the roles of Wnt/β-catenin signaling in cancers and provide insights to acknowledge the current opportunities and challenges of targeting this signaling in cancers.

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References
1.
Mizutani A, Yashiroda Y, Muramatsu Y, Yoshida H, Chikada T, Tsumura T . RK-287107, a potent and specific tankyrase inhibitor, blocks colorectal cancer cell growth in a preclinical model. Cancer Sci. 2018; 109(12):4003-4014. PMC: 6272098. DOI: 10.1111/cas.13805. View

2.
Aripaka K, Gudey S, Zang G, Schmidt A, Ahrling S, Osterman L . TRAF6 function as a novel co-regulator of Wnt3a target genes in prostate cancer. EBioMedicine. 2019; 45:192-207. PMC: 6642315. DOI: 10.1016/j.ebiom.2019.06.046. View

3.
Deng Y, Su Q, Mo J, Fu X, Zhang Y, Lin E . Celecoxib downregulates CD133 expression through inhibition of the Wnt signaling pathway in colon cancer cells. Cancer Invest. 2012; 31(2):97-102. DOI: 10.3109/07357907.2012.754458. View

4.
Yang Y, Zhao Z, Hou N, Li Y, Wang X, Wu F . MicroRNA‑214 targets Wnt3a to suppress liver cancer cell proliferation. Mol Med Rep. 2017; 16(5):6920-6927. DOI: 10.3892/mmr.2017.7483. View

5.
Chen Y, Li J, Yu X, Li S, Zhang X, Mo Z . APC gene hypermethylation and prostate cancer: a systematic review and meta-analysis. Eur J Hum Genet. 2013; 21(9):929-35. PMC: 3746257. DOI: 10.1038/ejhg.2012.281. View